NCT00917566

Brief Summary

This study indented to evaluate the use of Optical laryngoscope in pediatric

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
50

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Apr 2009

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 1, 2009

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

June 9, 2009

Completed
1 day until next milestone

First Posted

Study publicly available on registry

June 10, 2009

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2009

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2009

Completed
Last Updated

November 19, 2009

Status Verified

November 1, 2009

Enrollment Period

7 months

First QC Date

June 9, 2009

Last Update Submit

November 18, 2009

Conditions

Intubation

Keywords

AirtraqPediatric

Outcome Measures

Primary Outcomes (1)

  • Duration of intubation

    two minutes

Study Arms (2)

Airtraq group

ACTIVE COMPARATOR

Use Airtraq for intubation

Device: Airtraq

Macintoch gorup

ACTIVE COMPARATOR

Use Macintoch laryngoscope for intubation

Device: Macintoch

Interventions

AirtraqDEVICE

intubation with airtraq

Also known as: Optical laryngoscope
Airtraq group
MacintochDEVICE

use Macintoch laryngoscope for intubation

Also known as: Standard laryngoscope
Macintoch gorup

Eligibility Criteria

Age2 Years - 10 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17)

You may qualify if:

  • Healthy children undergoing general anesthesia required tracheal intubation.

You may not qualify if:

  • History of difficult intubation.
  • Risk of aspiration.
  • Children with cardiovascular disease.
  • Children with respiratory disease.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

king Khaled Eye Specialist hospital

Riyadh, Riyadh Region, 11462, Saudi Arabia

Location

Study Officials

  • Waleed Riad, MD, AB, SB

    King Khaled Eye Specialist Hospital

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER GOV

Study Record Dates

First Submitted

June 9, 2009

First Posted

June 10, 2009

Study Start

April 1, 2009

Primary Completion

November 1, 2009

Study Completion

November 1, 2009

Last Updated

November 19, 2009

Record last verified: 2009-11

Locations

SA(1)